lidocaine hydrochloride
Generic: lidocaine hydrochloride
Labeler: hf acquisition co llc, dba healthfirstDrug Facts
Product Profile
Brand Name
lidocaine hydrochloride
Generic Name
lidocaine hydrochloride
Labeler
hf acquisition co llc, dba healthfirst
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
lidocaine hydrochloride 20 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
51662-1454
Product ID
51662-1454_3310effb-5919-263a-e063-6394a90aba15
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA083158
Listing Expiration
2026-12-31
Marketing Start
2005-12-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516621454
Hyphenated Format
51662-1454
Supplemental Identifiers
RxCUI
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
lidocaine hydrochloride (source: ndc)
Generic Name
lidocaine hydrochloride (source: ndc)
Application Number
ANDA083158 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/mL
Packaging
- 5 mL in 1 SYRINGE (51662-1454-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "3310effb-5919-263a-e063-6394a90aba15", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1012068"], "spl_set_id": ["2177b6fe-aa37-6f6b-e063-6294a90af09a"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "5 mL in 1 SYRINGE (51662-1454-1)", "package_ndc": "51662-1454-1", "marketing_start_date": "20051201"}], "brand_name": "LIDOCAINE HYDROCHLORIDE", "product_id": "51662-1454_3310effb-5919-263a-e063-6394a90aba15", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "51662-1454", "generic_name": "LIDOCAINE HYDROCHLORIDE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LIDOCAINE HYDROCHLORIDE", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA083158", "marketing_category": "ANDA", "marketing_start_date": "20051201", "listing_expiration_date": "20261231"}